NDC 81119-002 Smile Antibacterial Wet Wipes D-panthenol
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What is NDC 81119-002?
What are the uses for Smile Antibacterial Wet Wipes D-panthenol?
Which are Smile Antibacterial Wet Wipes D-panthenol UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BENZALKONIUM (UNII: 7N6JUD5X6Y) (Active Moiety)
Which are Smile Antibacterial Wet Wipes D-panthenol Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PANTHENOL (UNII: WV9CM0O67Z)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- ETHYLPARABEN (UNII: 14255EXE39)
- BRONOPOL (UNII: 6PU1E16C9W)
- CETRIMONIUM BROMIDE (UNII: L64N7M9BWR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- PPG-2 METHYL ETHER (UNII: RQ1X8FMQ9N)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
What is the NDC to RxNorm Crosswalk for Smile Antibacterial Wet Wipes D-panthenol?
- RxCUI: 1038856 - benzalkonium Cl 0.1 % Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 1 MG/ML Medicated Pad
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Medicated Wipes
- RxCUI: 1038856 - benzalkonium chloride 0.1 % Topical Swab
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".